Results 111 to 120 of about 18,247 (232)
Scleroderma in South Australia: epidemiological observations of possible pathogenic significance.
BACKGROUND: Scleroderma is an autoimmune disorder of unknown cause. Previous epidemiological studies have suggested some regional clustering and associations with occupations involving exposure to silica dusts and hydrocarbons.
Kencana Dharmapatni, AA +15 more
core +1 more source
Ocular Manifestation in Systemic Sclerosis—A Literature Review
Systemic sclerosis (SSc) is a chronic autoimmune connective tissue disease that affects more than 2 million people worldwide. It manifests through vasculopathy, an abnormal immunological response, and fibrosis leading to dysfunction of the multiple ...
Katarzyna Paczwa +4 more
doaj +1 more source
In adult systemic sclerosis (SSc), salt-and-pepper skin changes can be used to diagnose diffuse cutaneous SSc during the early stages. However, reports of juvenile SSc (JSSc) with salt-and-pepper skin changes are unavailable.
Daisuke Hironaka +8 more
doaj +1 more source
Summary of Reported Cases of Nodular Scleroderma
Nodular (keloidal) Scleroderma (NS) constitutes a rare manifestation of cutaneous scleroderma, occurring either in conjunction with diffuse systemic sclerosis or as a localized form (morphea). The table summarizes the total number of NS cases reported in
Ntiri, M (via Mendeley Data)
core +1 more source
A cross-sectional comparison of three self-reported functional indices in scleroderma
Objectives. In scleroderma, outcome measures such as skin score provide only limited information about the functional impact of the disease. The requirement for validated and convenient instruments that reliably reflect disease morbidity is now ...
Black, C. M. +5 more
core +1 more source
Hutchinson-Gilford progeria syndrome (HGPS) is regarded as a model for aging. Moreover, the mutant protein accumulating in progeria is to some extent also found in healthy aged individuals.
Verstraeten, V. L.R.M.
core +1 more source
Background The overlap of non-cirrhotic idiopathic portal hypertension (NCIPH) and systemic sclerosis (SSc) is rare. This article reports one case of a patient with SSc developing NCIPH and presents a systematic review of previously reported cases ...
Felipe Souza da Silva +8 more
doaj +1 more source
Are we ready to predict progressive disease in juvenile systemic sclerosis? [PDF]
Foeldvari I, Klotsche J, Torok KS.
europepmc +1 more source
Diffuse fasciitis with eosinophilia. A clinicopathologic study
Three cases of diffuse fasciitis with eosinophilia are presented, and their clinical, laboratory and histologic follow-up are outlined. Furthermore histologic comparison with scleroderma is attempted and the literature is reviewed.
Shulman, L. E. +5 more
core
Pruritus associated with systemic sclerosis: a systematic review of treatment-based clinical trials. [PDF]
Mortezaei K +9 more
europepmc +1 more source

